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It is a diol that has hydroxyl groups (-OH) on vicinal carbon atoms. Disclaimer, Copyright © 2018 ChemSrc All Rights Reserved. We isolated three Sphingobium fuliginis strains from Phragmites australis rhizosphere sediment that were capable of utilizing 4-tert-butylphenol as a sole carbon and energy source. A novel carbonyl reductase with anti-Prelog stereospecificity from Acetobacter sp. Contact A novel carbonyl reductase (AcCR) catalyzing the asymmetric reduction of ketones to enantiopure alcohols with anti-Prelog stereoselectivity was found in Acetobacter sp. Boiling Point (°C) 101 - 200 (3) Melting Point (°C) less than 0 (1) Available for Sale. CCTCC M209061 and enriched 27.5... Appl. Liq.
All Rights Reserved. Initial Boiling Point: 106°C: Boiling Range: 106°C: Flash Point: 5°C: Relative Density: 0.801g/cm3: Other Information: No additional information available Download SDS.  It is also a controlled export in Australia Group member states. Product Result, Synonym:
tert-Butyl methyl ketone, Product Results, | Match Criteria: Property, Product Name, Synonym: Product Classification |
The fraction with boiling point 105 °C is the product. The molecule is an unsymmetrical ketone. Buying Leads |
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2A STOT SE 3: Signal Word: Danger: Pictograms: GHS02 GHS07: Hazards: H225 Highly flammable liquid and vapour. These strains are t... Biochem.
Environ. Soman (pinacolyl methylphosphonofluoridate), a highly toxic organophosphate compound, has been found to be a strong inhibitor of hepatic microsomal carboxylesterase in vitro, but an enhancer of carbox... Get all suppliers and price by the below link: Home |
CCTCC M209061: purification and characterization. Classification: Flam. pinacolone, 2 Pinacolone (3,3-dimethyl-2-butanone) is an important ketone in organic chemistry. Advanced Search | Structure Search.
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It is a colorless liquid and has a slight peppermint- or camphor- odor.
3-Methylbutanal is a starting material for 2,3-dimethyl-2-butene, which in turn is converted to pinacolone.
46(11) , 2083-92, (1993). | Privacy.
Boiling Point: 104.9±8.0 °C at 760 mmHg Vapour Pressure: 30.3±0.2 mmHg at 25°C Enthalpy of Vaporization: 33.4±0.0 kJ/mol Flash Point: 23.9±0.0 °C Index of Refraction: The molecule is an unsymmetrical ketone. Stable. (2,2-Dimethyl-1-methylenepropoxy)trimethylsilane,
Pinacolone (3,3-dimethyl-2-butanone) is an important ketone in organic chemistry.
1-Bromo-3,3-dimethyl-2-butanone, Articles of Pinacolone are included as well.
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Compare Products: Select up to 4 products. 3,3-Dimethyl-2-butanone. The α-methyl group can participate in condensation reactions. 2 Skin Irrit.
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The carbonyl group can undergo the usual reactions (hydrogenation, reductive amination, etc.). Pinacolone is produced in large amounts for use in fungicides, herbicides, and pesticides. Chemsrc provides Pinacolone(CAS#:75-97-8) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc.
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Incompatible with strong oxidizing agents. Pinacolone can also be produced from 2-methy-2-butanol when reacted with C5 alcohols.. Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter. Sorry we cannot compare more than 4 products at a time. Chemsrc provides Pinacolone(CAS#:75-97-8) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Boiling Point: 174.4±0.0 °C at 760 mmHg Vapour Pressure: 0.4±0.7 mmHg at 25°C Enthalpy of Vaporization: 47.8±6.0 kJ/mol Flash Point: 77.2±0.0 °C Index of Refraction: Pinacolone and pinacolyl alcohol produced enzyme enhancement in vitro in a manner similar to that produced by soman pretreatment.
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These effects were compared with those made by acetone in the same incubations, since the enhancing influence of acetone has already been well documented.
2 Eye Irrit. Bromomethyl tert-butyl ketone. It also is generated by ketonization of pivalic acid and acetic acid or acetone over metal oxide catalysts. Articles of Pinacolone are included as well.
The α-methyl group can participate in condensation reactions. , Industrially pinacolone is made by the hydrolysis of 4,4,5-trimethyl-1,3-dioxane, which is the product of isoprene and formaldehyde via the Prins reaction. H315 Causes skin irritation. matches found for α,α,α-Trimethylacetone, Isolation and characterization of 4-tert-butylphenol-utilizing Sphingobium fuliginis strains from Phragmites australis rhizosphere sediment. Flammable. Biologically Active Compounds |
It is a precursor to triazolylpinacolone in the synthesis of the fungicide triadimefon and in synthesis of the herbicide metribuzin. Customer Service. 5 matches found for pinacolone. It is a Schedule 3 compound under the Chemical Weapons Convention 1993, due to being related to pinacolyl alcohol, which is used in the production of soman.